About this trial
This study investigates whether the activity of brown adipose tissue (BAT) - a special type of fat that burns energy as heat - can predict how well individuals with obesity respond to semaglutide (Wegovy), a once-weekly injectable weight loss medication. Participants who are starting semaglutide treatment will undergo ¹⁸FDG-PET/CT imaging before and after 24 weeks of treatment. Prior to each PET/CT scan, participants will wear a water-circulating cooling vest to activate BAT. By measuring BAT activity at baseline and comparing it with the degree of weight loss and metabolic improvement at 24 weeks, the investigators aim to identify BAT as a predictive biomarker for personalized obesity treatment.
Eligibility criteria
Qualifiers
Age 20-70 years at the time of enrollment
Initiating semaglutide (Wegovy) treatment for obesity (newly starting treatment)
Hypertension (SBP ≥130 or DBP ≥80 mmHg, or on antihypertensive medication)
Dyslipidemia (LDL-C ≥130, TG ≥150, or low HDL-C, or on lipid-lowering medication)
Disqualifiers
Diagnosis of type 1 or type 2 diabetes mellitus
History of neck surgery or radiation therapy to the neck
Use of anti-obesity medications within 1 month prior to enrollment, or current use of beta-adrenergic blocking agents
Personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2 (MEN2)
Trial design
Treatments tested in this trial
- Semaglutide (Wegovy®)
- ¹⁸FDG-PET/CT with cold stimulation
- Liver MRI (PDFF + MRE)
Treatment groups
Locations
2Sponsors and collaborators
Hallym University
Lead sponsor
Hallym University Dongtan Sacred Heart Hospital
Sponsor institution
Hallym University Dongtan Sacred Heart Hospital
Collaborator